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Human Induced Pluripotent Stem Cell-Derived Cardiac Cell Sheets Expressing Genetically Encoded Voltage Indicator for Pharmacological and Arrhythmia Studies

机译:人类诱导的多能干细胞衍生的心脏细胞片表达遗传编码的电压指示剂,用于药理和心律失常研究

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Summary Fulfilling the potential of human induced pluripotent stem cell (hiPSC)-derived cardiomyocytes for studying conduction and arrhythmogenesis requires development of multicellular models and methods for long-term repeated tissue phenotyping. We generated confluent hiPSC-derived cardiac cell sheets (hiPSC-CCSs), expressing the genetically encoded voltage indicator ArcLight. ArcLight-based optical mapping allowed generation of activation and action-potential duration (APD) maps, which were validated by mapping the same hiPSC-CCSs with the voltage-sensitive dye, Di-4-ANBDQBS. ArcLight mapping allowed long-term assessment of electrical remodeling in the hiPSC-CCSs and evaluation of drug-induced conduction slowing (carbenoxolone, lidocaine, and quinidine) and APD prolongation (quinidine and dofetilide). The latter studies also enabled step-by-step depiction of drug-induced arrhythmogenesis ("torsades de pointes in the culture dish") and its prevention by MgSO4 and rapid pacing. Phase-mapping analysis allowed biophysical characterization of spiral waves induced in the hiPSC-CCSs and their termination by electrical cardioversion and overdrive pacing. In conclusion, ArcLight mapping of hiPSC-CCSs provides a powerful tool for drug testing and arrhythmia investigation.
机译:总结要发挥人类诱导的多能干细胞(hiPSC)衍生的心肌细胞研究传导和心律不齐的潜力,就需要开发用于长期重复组织表型的多细胞模型和方法。我们生成了融合的hiPSC衍生的心脏细胞表(hiPSC-CCSs),表达了遗传编码的电压指示器ArcLight。基于ArcLight的光学映射可以生成激活图和动作电位持续时间(APD)图,这可以通过将相同的hiPSC-CCS与压敏染料Di-4-ANBDQBS映射来验证。 ArcLight映射可以对hiPSC-CCS中的电重构进行长期评估,并可以评估药物引起的传导减慢(卡培诺酮,利多卡因和奎尼丁)和APD延长(奎尼丁和多非利特)。后者的研究还可以逐步描述药物引起的心律失常(“培养皿中的尖尖扭转”)及其通过MgSO 4 和快速起搏的预防作用。相图分析可以对hiPSC-CCS中诱导的螺旋波进行生物物理表征,并通过电复律和超速起搏来终止螺旋波。总之,hiPSC-CCS的ArcLight映射为药物测试和心律失常研究提供了强大的工具。

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